237653008: Familial primary hyperparathyroidism (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of neck region\Disease of neck\Disorder of parathyroid gland (disorder)\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism

\Functional finding\Increased hormone secretion\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism

\Endocrine finding\Increased hormone secretion\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism

\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of parathyroid gland (disorder)\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism
\Disease\Disease of neck\Disorder of parathyroid gland (disorder)\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

356183018 Familial hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356184012 Familial primary hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626412019 Familial primary hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

356183018 Familial hyperparathyroidism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356183018 Familial hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356184012 Familial primary hyperparathyroidism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356184012 Familial primary hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626412019 Familial primary hyperparathyroidism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626412019 Familial primary hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3441041001000111 Hyperparathyreoidismus, familiärer primärer de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

918921000172112 hyperparathyroïdie primitive familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

918921000172112 hyperparathyroïdie primitive familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3441041001000111 Hyperparathyreoidismus, familiärer primärer de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial hyperparathyroidism	Is a	Primary hyperparathyroidism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hyperparathyroidism	Finding site	Parathyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial hyperparathyroidism	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hyperparathyroidism	Has definitional manifestation	Increased hormone secretion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hyperparathyroidism	Has interpretation	Increased	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial hyperparathyroidism	Interprets	Hormone secretion	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hyperparathyroidism-jaw tumor syndrome (disorder)	Is a	True	Familial hyperparathyroidism	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumours in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumours and/or systemic manifestations.	Is a	True	Familial hyperparathyroidism	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets